Evidence map›Paper›PMID 32090454›Full record

ArticleJournal of cellular and molecular medicine2020

Arctigenin prevents the progression of osteoarthritis by targeting PI3K/Akt/NF-κB axis: In vitro and in vivo studies.

Shangkun Tang, Weijun Zhou, Xinyang Zhong, Jianchen Xu, Huasong Huang, Xinnan Zheng, Jingkang Zhang, Shuyue Yang, Ping Shang, Qian Tang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 22 citations in OpenAlex.

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  11. An Overview of NO Signaling Pathways in Aging.Molecules (Basel, Switzerland) · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Shangkun TangDepartment of Orthopaedic Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Weijun ZhouDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Xinyang ZhongDepartment of Orthopaedic Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Jianchen XuDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Huasong HuangDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Xinnan ZhengDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Jingkang ZhangDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Shuyue YangDepartment of Clinical Medicine, Second Clinical Medical College, Wenzhou Medical University, Wenzhou, China.
Ping ShangDepartment of Rehabilitation, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Qian TangDepartment of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Haixiao LiuDepartment of Orthopaedic Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.ORCID 0000-0003-0994-2005
Wenzhou Medical University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA), which is principally featured by progressive joint metabolic imbalance and subsequent degeneration of articular cartilage, is a common chronic joint disease. Arctigenin (ATG), a dietary phyto-oestrogen, has been described to have potent anti-inflammatory effects. Nevertheless, its protective effects on OA have not been clearly established. The target of our following study is to evaluate the protective effects of ATG on IL-1β-induced human OA chondrocytes and mouse OA model. Our results revealed that the ATG pre-treatment effectively decreases the level of pro-inflammatory mediators, such as prostaglandin E2 (PGE2), nitrous oxide (NO), inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), IL-6 and tumour necrosis factor alpha (TNF-α) in IL-1β-induced human chondrocytes. In addition, ATG protects against the degradation of extracellular matrix (ECM) under the stimulation of IL-1β and the possible mechanism might be connected with the inactivation of phosphatidylinositol-3-kinase (PI3K)/Akt/nuclear factor-kappa B (NF-κB) axis. Furthermore, a powerful binding capacity between ATG and PI3K was also uncovered in our molecular docking research. Meanwhile, ATG may act as a protector on the mouse OA model. Collectively, all these findings suggest that ATG could be utilized as a promising therapeutic agent for the treatment of OA.

Indexed as

AnimalsCartilage, ArticularChondrocytesDinoprostoneDisease Models, AnimalDisease ProgressionFuransHumansInflammationInterleukin-1betaInterleukin-6LignansMiceMolecular Docking SimulationNF-kappa BNitric Oxide Synthase Type IIarctigeninDinoprostoneFuransIL1B protein, humanInterleukin-1betaInterleukin-6LignansNF-kappa BNitric Oxide Synthase Type IINitrous OxideNOS2 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktarctigeninchondrocyteinflammationNF-κBosteoarthritis

Identifiers

PMID32090454
PMCPMC7171400
OpenAlexW3007955016

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.